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rs267606909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606909(A;A)
Make rs267606909(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23415258
GeneMYH7
is asnp
is mentioned by
dbSNPrs267606909
ebirs267606909
HLIrs267606909
Exacrs267606909
Varsomers267606909
Maprs267606909
PheGenIrs267606909
hapmaprs267606909
1000 genomesrs267606909
hgdprs267606909
ensemblrs267606909
gopubmedrs267606909
geneviewrs267606909
scholarrs267606909
googlers267606909
pharmgkbrs267606909
gwascentralrs267606909
openSNPrs267606909
23andMers267606909
23andMe allrs267606909
SNP Nexus

SNPshotrs267606909
SNPdbers267606909
MSV3drs267606909
GWAS Ctlgrs267606909
Max Magnitude0
ClinVar
Risk rs267606909(A;A)
Alt rs267606909(A;A)
Reference rs267606909(G;G)
Significance Pathogenic
Disease Left ventricular noncompaction 5
Variation info
Gene MYH7 MHRT
CLNDBN Left ventricular noncompaction 5
Reversed 1
HGVS NC_000014.8:g.23884467C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015189.25,